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About This Item
Empirical Formula (Hill Notation):
C15H10O3
CAS Number:
Molecular Weight:
238.24
EC Number:
209-416-9
UNSPSC Code:
12352100
MDL number:
assay
99%
mp
171-172 °C (lit.)
SMILES string
OC1=C(Oc2ccccc2C1=O)c3ccccc3
InChI
1S/C15H10O3/c16-13-11-8-4-5-9-12(11)18-15(14(13)17)10-6-2-1-3-7-10/h1-9,17H
InChI key
HVQAJTFOCKOKIN-UHFFFAOYSA-N
Application
Reactant involved in:
Reactant involved in the synthesis of biologically active molecules including:
Involved in studies of its electrochemical properties using voltammetric methodologies
- Studies of photochemically-induced dioxygenase-type CO-release reactivity
- Phase-transfer protection and deprotection of hydroxychromones
- O-methylation with di-Me carbonate
Reactant involved in the synthesis of biologically active molecules including:
- 2-Chloropyridine derivatives for studies of antitumor agents and telomerase inhibitors
- Dihydrochromenopyrazines and chromenoquinoxalines
Involved in studies of its electrochemical properties using voltammetric methodologies
Regulatory Information
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Aik Jiang Lau et al.
Pharmacological research, 100, 64-72 (2015-08-05)
Pregnane X receptor (PXR; NR1I2) is a member of the superfamily of nuclear receptors that regulates the expression of genes involved in various biological processes, including drug transport and biotransformation. In the present study, we investigated the effect of 3-hydroxyflavone